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GPATCH11

Gene

G-patch domain containing 11

HGNCHGNC:26768EnsemblENSG00000152133NCBI Gene253635
Locus: gene with protein productLocation: 2p22.2

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asCCDC75 · FLJ38348 · CENPY · CENP-Y
View full nomenclature history (6)
Previous symbolsCCDC75
Alias symbolsFLJ38348, CENPY, CENP-Y
Previous namescoiled-coil domain containing 75
Alias namescentromere protein Y

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Neurodevelopmental Disorders
Head and Neck Neoplasms
Lupus Erythematosus, Systemic
Retinal Diseases
Gout
Multiple Sclerosis
Heart Failure
Diabetes Mellitus, Type 2
Atrial Fibrillation

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

G-patch domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.